Nur77 Signaling in T-Cell

No Pathway Network information available for Nur77 Signaling in T-Cell

Pathways in the Nur77 Signaling in T-Cell SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Nur77 Signaling in T-Cell SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E7.80
2Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM1, CALM2, CALM36.06
3Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G5.84
4Witteveen-kolk syndromeEnrichmentSIN3A, SIN3B5.19
5Long qt syndrome 1EnrichmentCALM1, CALM2, CALM34.22
6Auriculocondylar syndrome 4EnrichmentHDAC92.59
7Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.59
8Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.59
9Immunodeficiency 18EnrichmentCD3E2.59
10Immunodeficiency 25EnrichmentCD2472.59
11Thrombocytopenia 4EnrichmentCYCS2.59
12Long qt syndrome 16EnrichmentCALM32.59
13Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.59
14Immunodeficiency 19, severe combinedEnrichmentCD3D2.59
15Long qt syndrome 15EnrichmentCALM22.59
16Chromosome 15q24 deletion syndromeEnrichmentSIN3A2.59
17Cerebral cavernous malformations 5EnrichmentMAP3K32.59
18Immunodeficiency 19EnrichmentCD3D2.59
19Verrucous hemangiomaEnrichmentMAP3K32.59
20Long qt syndromeEnrichmentCALM1, CALM22.54
21Scoliosis, isolated 1EnrichmentMAPK72.29
22Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM12.29
23Long qt syndrome 14EnrichmentCALM12.29
24Menke-hennekam syndrome 2EnrichmentEP3002.29
25Intravascular large b-cell lymphomaEnrichmentBCL22.29
26Immunodeficiency 17EnrichmentCD3G2.29
27Mycosis fungoidesEnrichmentCD282.11
28High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.11
29Saczary syndromeEnrichmentCD282.11
30Rubinstein-taybi syndrome 2EnrichmentEP3001.89
31Follicular lymphomaEnrichmentBCL21.89
32Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.89
33Rubinstein-taybi syndrome 1EnrichmentEP3001.81
34Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.81
35Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.81
36Oligoarticular juvenile idiopathic arthritisEnrichmentCD2471.75
37Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD2471.75
38Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.69
39Charge syndromeEnrichmentEP3001.64
40Polydactyly, postaxial, type a1EnrichmentEP3001.42
41Rare genetic intellectual disabilityEnrichmentEP3001.42
42Sudden infant death syndromeEnrichmentCALM21.37
43ThrombocytopeniaEnrichmentCYCS0.93
44Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.92
45Myeloma, multipleEnrichmentRXRA0.87
46Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.87
47Colorectal cancerEnrichmentEP3000.69
48MicrocephalyEnrichmentEP3000.56

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